R7G (p.Arg7Gly) variant of BRCA1 (P38398)
R7G (p.Arg7Gly) in BRCA1 (P38398) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes experimental measurements, published literature, and structural context.
R7G (p.Arg7Gly) variant details
- p.Arg7Gly
- rs80356994
- ClinGen CA10602123
- ClinVar RCV001078112
- ESP rs80356994
- Likely benign
- Missense
- Variant Prioritization Score for Impact Estimate 0.438
- AlphaMissense 0.24
- MetaLR 0.40
- MetaSVM -0.50
- PolyPhen-2 0.21
- SIFT 0.73
- EVE 0.22
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available
- BRCA1 SGE Exon 2 Replicate 2: score -1.33
- Cited in: Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. (PMID 15604628)
- Cited in: American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography. (PMID 17392385)